Effect of volume of distension fluid for capsular dilatation under ultrasound guided in patient with adhesive capsulitis; A double blind randomized controlled trial
Phase 1
Recruiting
- Conditions
- patient with adhesive capsulitisadhesive capsulitis, intra articular injection, hydrodilatation
- Registration Number
- TCTR20240515005
- Lead Sponsor
- Phramongkutklao hospital research fund
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 54
Inclusion Criteria
VAS score of shoulder >= 4
and
limit AROM or PROM at least 2 direction
symptom more than a month
Exclusion Criteria
Full thickness tear of rotator cuff
has previous intra-articular injection within 3 month
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual analog scale (VAS) at 1st visit, 1 month and 6 month pain measurement (objective)
- Secondary Outcome Measures
Name Time Method Range of motion at 1st visit, 1 month and 6 month goniometer,Shoulder Pain and Disability Index at 1st visit, 1 month and 6 month pain assessment